Barley with reduced SSII activity and starch containing products with a reduced amylopectin content

ABSTRACT

Barley with reduced SSII activity has a starch structure with reduced amylopectin content and a consequent high relative amylose content. Additionally the grain can have a relatively high β glucan content. The structure of the starch may also be altered in a number of ways which can be characterized by having a low gelatinsation temperature but with reduced swelling. The viscosity of gelatinised starch of the starch is also reduced. There is a chain length distribution of the amylopectin content and a low crystallinity of the starch. The starch is also characterized by having high levels of lipid associated starch exhibiting very high levels of V form starch crystallinity. The dietary fiber content of the starch is high. This has desirable dietary and food processing characteristics.

This invention relates to a barley plant with a reduced SSII enzyme activity leading to a starch having reduced amylopectin content. The invention also relates to starch and grain and food products obtained therefrom.

BACKGROUND OF THE INVENTION

One finding in nutritional science is that resistant starch has important implications for bowel health, in particular health of the large bowel. The beneficial effects of resistant starch result from the provision of a nutrient to the large bowel wherein the intestinal microflora are given an energy source which is fermented to form inter alia short chain fatty acids. These short chain fatty acids provide nutrients for the colonocytes, enhance the uptake of certain nutrients across the large bowel and promote physiological activity of the colon. Generally if resistant starches or other dietary fibre is not provided the colon is metabolically relatively inactive.

There has in recent years been a direction to look at providing for resistant starches from various sources to address bowel health. Accordingly high amylose starches have been developed in certain grains such as maize for use in foods as a means of promoting bowel health.

The physical structure of starch can have an important impact on the nutritional and handling properties of starch for food products. Certain characteristics can be taken as an indication of starch structure including the distribution of amylopectin chain length, the degree of crystallinity and the presence of forms of crystallinity such as the V-complex form of starch crystallinity. Forms of these characteristics can also be taken as indicator of nutritional or handling properties of foods containing these starches. Thus short amylopectin chain length may be an indicator of low crystallinity and low gelatinisation and is also thought to have a correlation with reduced retrogradation of amylopectin. Additionally shorter amylopectin chain length distribution is thought to reflect organoleptic properties of food in which the starch is included in significant amounts. Reduced crystallinity of a starch may also be indicative of a reduced gelatinisation temperature of starch and additionally it is thought to be associated with enhanced organoleptic properties. The presence of V-complex crystallinity or other starch associated lipid will enhance the level of resistant starch and thus dietary fibre.

Lines of barley having high amylose starch contents have been identified in the past. These have only resulted in relatively modest increases in amylose content to a maximum of about 45% of total starch such as in the barley variety known as High Amylose Glacier (AC38). Whilst elevated amylose starches of that type are useful a starch with a higher amylose content still is preferred, and certain other species of grain are bred to have higher amylose content starches with levels in the 90 percentile range. These are very resistant to digestion and bring a greater health benefit.

There is a problem with providing the high amylose starches because known high amylose starches also have a high gelatinisation temperature. Gelatinisation temperature is reflective of the comminution energy required to process such foods. Thus higher temperatures are normally required to process grain or flour to manufacture foods from such grains or starches. Thus generally products having high amylose starches are more expensive. Similarly from the point of view of the consumer longer times and higher temperatures may be required to prepare the manufactured foods, or to make foods from flour having high amylose starches. Thus there is a significant disadvantage in the provision of high amylose starches in foods.

Another nutritional component of the grains and in particular of barley as β-glucans. β-glucans consist of glucose units bonded by β (1-4) and/or β (1-3) glycosidic linkages and are also not degraded by human digestive enzymes which makes them suitable as a source of dietary fibre. β-glucans can be partially digested by endogenous colonic bacteria which fermentation process gives rise to short chain fatty acids (predominantly acetate, propionate and butyrate) which are beneficial to mucosal cells lining the intestine and colon (Sakata and Engelhard Comp. Biochem Physiol. 74a:459-462 (1983))

Ingestion of β-glucan also has the effect of increasing bile acid excretion leading to a reduction in total serum cholesterol and low density lipoproteins (LDL) with a lowering of the risk of coronary disease. Similarly β-glucans act by attenuating excursions in postprandial blood glucose concentration. It is thought that both of these effects are based on the increase of viscosity in the contents of the stomach and intestines.

The composition of foods containing starches and the intimate relationship of those starches with other nutritional or other components can have a significant impact on the nutritional value of those foods or on the functional characteristics of those components in the preparation or structure of the foods.

Whilst modified starches or β glucans, for example, can be utilised in foods that provide functionality not normally afforded by unmodified sources, such processing has a tendency to either alter other components of value or carry the perception of being undesirable due to processes involved in modification. Therefore it is preferable to provide sources of constituents that can be used in unmodified form in foods.

The barley variety MK6827 is available from the Barley Germplasma Collection (USDA-ARS National Small Grain Germplasma Research Facility Aberdeen, Id. 831290 USA). The grain of MK6827 is shrunken and has a highly coloured husk and an elongate shape and, in the hands of the inventors, this grain is very difficult to process including being very resistant to milling. The properties of MK6827 grain had not been characterised before, nor had the nature of the mutation been ascertained nor is it considered suitable for producing food.

SUMMARY OF THE INVENTION

This invention arises from the isolation and characterisation of SSII mutant of barley plants the grain of which is found to contain starch that has reduced amylopectin content and therefore high relative levels of amylose and therefore has elevated levels of dietary fibre.

The grain of the mutant and grain from crosses into certain genetic backgrounds additionally has an elevated level of β glucan. The combination of elevated β glucan level and resistant starch contributing to high dietary fibre is thought by the inventors to be unique to the present invention.

Additionally, at least in some genetic backgrounds, it is found that grain from such mutants contain starch that have high relative levels of amylose, and also have low gelatinisation temperatures. The low swelling charactistics of such starch during and following gelatinisation also has advantages in certain dietary and food processing applications.

Furthermore, grain from such mutants are found to contain starch that have high relative levels of amylose, the amylose levels found are higher than 50% of the starch content which is a level never before found in unmodified starch derived from barley.

The starch of the mutants and backcrossed lines derived from the mutants (to the extent that the backcrosses have been tested) exhibit a resistant starch, with an altered structure indicated by specific physical characteristics including one or more of the group comprising the presence of a high relative amylose content, physical inaccessibility by reason of having a high β-glucan content, altered granule morphology, and the presence of starch associated lipid, and the altered structure being indicated by a characteristic selected from one or more of the group comprising low crystallinity, reduced amylopectin chain length distribution and presence of appreciable starch associated lipid.

Additionally thus far the grain derived from the mutant barley plants can readily be used in food processing procedures.

This invention in one aspect might be said to reside in starch obtained from the of grain of a barley plant the barley plant having a reduced level of SSII activity, said starch granules having a high amylose content by reason of a reduced amylopectin content.

The invention might in another aspect of broadly be said to reside a grain useful for food production obtained from a barley plant the barley plant having a reduced level of SSII activity, starch of said grain having a high amylose content by reason of a reduced amylopectin content.

In a yet further aspect the invention might broadly said to reside in a barley plant with a reduced level of SSII activity, said barley plant capable of bearing grain, starch of said grain having a high amylose content by reason of a reduced amylopectin content, said grain suitable for food production.

Alternatively the invention could be said to reside in an isolated nucleic acid molecule encoding a barley SSII protein said nucleic acid capable of hybridising under stringent conditions with SEQ ID NO 1. or a cell carrying a replicable recombinant vector carrying said nucleic acid molecule. In a yet further form the invention might be isolated nucleic acid molecule capable of hybridising specifically to SEQ ID NO 1.

BRIEF DESCRIPTION OF THE DRAWINGS

For a better understanding, the invention will now be described with reference to a number of examples.

FIG. 1 Analysis of the starch molecular size distribution as determined by HPLC separation of starch in 90% DMSO. (a) Himalaya (b) AC38 (c) 342 (d) 292

FIG. 2 Photographs showing the grain morphology of mutant and parental lines. (a) Himalaya (b) AC38 (c) 292 (d) Waxiro (e) 342 (f) Tantangara (g) MK6827 (h) Sloop. The length (L), width (W) and thickness (T) dimensions of the grain are illustrated in panel (a).

FIG. 3 Analysis of the chain length distribution of various mutant and wild type starches using FACE. (a) normalised chain length distribution (b) comparison of chain length distributions by difference plot. Samples were 342 (▪), 292 (●), Tantangara (s), AC38 (

), MK6827 (♦) and Himalaya (+).

FIG. 4 RVA analysis of barley starch samples. Samples were Himalaya (

), Namoi (Δ), AC38 (◯), 342 (∇), 292 (▴) and MK6827 (▪). The temperature profile used during the profile is indicated by the unbroken line.

FIG. 5 X-ray diffraction data for mutant and wild type lines.

FIG. 6 Scanning electron micrographs of isolated barley starches. (a) Himalaya (b) Waxiro (c) AC38 (d) 292 (e) 342 (f) MK6827

FIG. 7. Loci on barley chromosome 7H showing the proximity of the nud1 and sex6 loci. Diagram after GrainGenes (http://wheat.pw.usda.gov/) Barley morphological genes, 7H map, author; Franckowiak J D.

FIG. 8. Relationships between seed dimensions and starch chain length distribution for 292× Tantangara doubled haploid lines. Lines denoted by (+) yielded the Himalaya PCR pattern and lines denoted by (◯) gave the 292 PCR result. Panel (A), the seed length to thickness ratio plotted against the percentage of starch chains with DP between 6 and 11; Panel (B) seed weight plotted against the percentage of starch chains with DP between 6 and 11

FIG. 9 Sequence of a barley SSII cDNA (SEQ ID NO 1) from the cultivar Himalaya

FIG. 10 The structure of the SSII genes from (1) T. tauschii (diploid wheat), (2) barley cultivar Morex. The thick lines represent exons and the thin lines introns. The straight line underneath each example indicates the region of the gene sequences. The dotted line represents a region of the barley SSII gene, from intron 7, that has not been sequenced but has been determined by PCR analysis to be approximately 3 kb in length.

FIG. 11 Comparisons of the predicted SSII cDNAs from MK6827 (SEQ ID NO 2), Morex (SEQ ID NO 3) and 292 (SEQ ID NO 4), and a cDNA sequence of Himalaya (SEQ ID NO 1). Predicted sequences were generated by identifying regions of the genomic sequences present in the Himalaya SSII cDNA. The ATG start codon and wild type stop codon are indicated, as are additional stop codons present in MK6827 (#) and 292 (&) respectively.

FIG. 12 Comparison of amino acid sequences deduced from the genes encoding SSII from barley lines 292 (SEQ ID NO 7 and SEQ ID NO 8), Morex (SEQ ID NO 5), MK6827 (SEQ ID NO 9 and SEQ ID NO 10), Himalaya (SEQ ID NO 6). Additional stop codons in 292 and MK6827 are indicated by the symbols (&) and (#) respectively.

FIG. 13. Position of the mutations in MK6827 (SEQ ID NO 2) and 292 (SEQ ID NO 4) in the barley SSII gene.

FIG. 14. Development and use of a PCR assay for the 292 mutation. (a) schematic representation of an SSII region from Himalaya amplified by the primers ZLSS2P4 and ZLBSSIIP5 (b) representation of the region amplified from the SSII gene from 292 using ZLSS2P4 and ZLBSSIIP5, showing the absence of one NlaIV site (c) agarose gel electrophoresis of NlaIV digested products from barley; Lane M; DNA marker ladder, lane 1: MK6827, lane 2; Himalaya; lane 3, Tantangara; lane 4, 292; lane 5, 342.

FIG. 15. A schematic representation of DNA constructs designed to down regulate SSII expression following stable transformation of barley (1). The SSII gene from nucleotides 1 to 2972 (See FIG. 9 for sequence) is inserted between the promoter and terminator in the sense orientation. (2) The SSII gene is inserted between the promoter an terminator in the anti-sense orientation from nucleotides 2972 to 1 (see FIG. 9 for sequence). (3) Duplex construct in which intron 3 of the barley SSII gene (between nucleotides 1559 and 2851) of the Morex SSII genomic sequence is inserted between exons 2 and 3 from the barley SSII cDNA from Himalaya (nucleotides 363 to 1157 from FIG. 9).

FIG. 16 SDS-PAGE electrophoresis of starch granule proteins. Panel (A) 8% Acrylamide (37.5:1 Acryl/Bis) SDS-PAGE gel, electroblotted and probed with a SSII antibody produced against purified granule-bound SSII protein from Wheat. (B) 12.5% acrylamide (30:0.135 Acryl/Bis), silver stained. The migration of molecular weight standards of defined mass (units are kd) are indicated on each side of the figure.

DETAILED DESCRIPTION OF THE INVENTION

Definitions

Glycaemic Index. Is a comparison of the effect of a test food such as white bread or glucose on excursions in blood glucose concentration. The Glycaemic Index is a measure of the likely effect of the food concerned on post prandial serum glucose concentration and demand for insulin for blood glucose homeostasis.

Resistant Starch. The sum of starch and products of starch digestion not absorbed in the small intestine of healthy humans but entering into the large bowel. Thus resistant starch excludes products digested and absorbed in the small intestine.

Resistant starches can be classified in four groups.

-   -   RS1 physically inaccessible starch. Examples of this form of         starch arise where the starch is entrapped within a protein or         similar matrix or within plant cell wall, or might arise because         of the partial milling of grain or in legumes after cooling.     -   RS2 Resistant granules. These are generally raw starches such as         those that arise from raw potato or green banana, some legumes         and high amylose starches.     -   RS3 Retrograded starches. These arise by heat/moisture treatment         of starch or starch foods such as occurs in cooked and cooled         potato, bread and cornflakes.     -   RS4 Chemically modified. These arise by reason of chemical         modifications such as substitution or cross linking. This form         of starch is often used in processed foods.

Dietary fibre. In this specification is the sum of carbohydrates or carbohydrate digestion products that is not absorbed in the small intestine of healthy humans but enters the large bowel. This includes resistant starch, β-glucan and other soluble and insoluble carbohydrate polymers. It is intended to comprise that portion of carbohydrates that are fermentable, at least partially, in the large bowel by the resident microflora.

Gelatinsation is the collapse (disruption) of molecular order within the starch granule with concomitant and irreversible changes in properties such as granular swelling, crystallite melting, loss of birefringence, viscosity development and starch solubilisation.

This invention arises from the isolation and characterisation of SSII mutant barley plants the grain of which is found to contain starch that has reduced amylopectin content and therefore high relative levels of amylose and therefore has elevated levels of dietary fibre.

Such mutants are found to have a number of quite desirable characteristics, and it has been shown that crosses into various other genetic backgrounds maintains at least some of those characteristics.

The grain of the mutant and grain from crosses into certain genetic backgrounds additionally has an elevated level of β glucan. The combination of elevated β glucan level and high dietary fibre is thought by the inventors to be unique to the present invention.

Additionally at least in some genetic backgrounds it is found that grain from such mutants are found to contain starch that have high relative levels of amylose, and also have low gelatinisation temperatures. The swelling charactistics of the gelatinisation of such starch also has the benefit of being low swelling which has advantages in certain dietary and food processing applications.

Furthermore grain from such mutants are found to contain starch that have high relative levels of amylose, the amylose levels found are higher than 50% of the starch content which is a level never before found in unmodified starch derived from barley.

The starch of the mutants and to the extent that the backcrosses have been tested exhibit a resistant starch, with an altered structure indicated by specific physical characteristics including one or more of the group comprising the presence of a high relative amylose content, physical inaccessibility by reason of having a high β-glucan content, altered granule morphology, and the presence of starch associated lipid, and the altered structure being indicated by a characteristic selected from one or more of the group comprising low crystallinity, reduced amylopectin chain length distribution and presence of appreciable starch associated lipid.

Additionally thus far the grain derived from the mutant barley plants can readily be used in food processing procedures.

Grain from such mutants in one form preferably contain starch that have high relative levels of dietary fibre, more particularly amylose as well as an elevated level of β glucan. The combination of elevated β glucan level and high amylose level is thought by the inventors to be unique to the present invention, and provide for a unique source of a combination of β-glucan and resistant starch that does not, at least in broader forms of the invention require mixing of β glucan and soluble dietary fibre together or modification of the component parts.

To the best of the knowledge of the inventors the barley plant of the present invention is the first time that there has been a barley grain having elevated relative dietary fibre levels in the form of resistant starch having an elevated amylose level, that also has elevated levels of β glucan that are at the higher end of the typical levels of β glucan or that go beyond that level. Grains that have β glucan content that are still higher are of the waxy phenotype and therefore have low levels of amylose.

It is known that there is a wide variation in β glucan levels in barley in the range of about 4% to about 18% by weight of the barley, but more typically from 4% to about 8% (Izydorcyk et al., (2000) Journal of Agricultural and Food Chemistry 48, 982-989; Zheng et al., (2000) Cereal Chemistry 77, 140-144; Elfverson et al., (1999) Cereal Chemistry 76, 434-438; Andersson et al., (1999) Journal of the Science of Foods and Agriculture 79, 979-986; Oscarsson et al., (1996) J Cereal Science 24, 161-170; Fastnaught et al., (1996) Crop Science 36, 941-946). Enhanced barley strains have been developed, Prowashonupana for example, which have between about 15% and about 18% by weight β-glucan but has a waxy phenotype. This is sold commercially under the name Sustagrain™, (ConAgra™ Specially Grain Products Company, Omaha, Nebr. USA).

The levels of β glucan contemplated by this invention may depend on the genetic background in which the amylopectin synthesis enzyme activity is reduced. However it is proposed that the reduction of the amylopectin synthesis activity will have the effect of elevating the relative level of dietary fibre which, in part, takes the form of amylose, and at the same time elevating the level of β glucan. One explanation for the concomitant elevation of β glucan with elevated relative amylose levels is that such elevation might be the result of a concentration effect of having reduced endosperm and may be further increased through the diversion of carbon from starch synthesis to β glucan synthesis.

Thus the grain of the barley plant preferably has a β glucan content that is greater than 6% of total non-hulled grain weight or more preferably greater than 7% and most preferably greater than 8%, however levels of β glucan in a waxy mutant has been measured as being as high as 15 to 18% and the present invention may contemplate levels as high, or higher, than that.

In a second preferable form the grain of the barley plant has a reduced gelatinsation temperature (as measured by differential scanning calorimetry)in addition to the relatively high amylose content. On the data shown for the exemplified barley this reduced gelatinisation temperature is not just reduced when compared to starch produced by barley with somewhat elevated amylose content but also when compared with starch produced from barley with starch having normal levels of amylose. Thus whilst the invention contemplates reduced gelatinisation temperatures relative to a corresponding high amylose starch, it may also contemplate a gelatinisation temperature reduced relative to that of starch with normal amylose levels.

Additionally in the genetic backgrounds thus far checked the starch is also characterised by a swelling in heated excess water that is lower than swelling of other starches tested.

In a third preferable form the starch has amylose levels of higher than 50% of the starch content which is a level never before found in unmodified starch derived from barley.

The starch of the present barley plant has a high relative amylose content and much higher than might be anticipated for a mutation in the SSII gene or other starch synthase gene. Thus in wheat mutants in SSII result in relative amylose levels of about 35% of starch. The amylose content of starch might be considered to be elevated when the content is significantly greater than the 25% or so that is present in normal barley grain and thus might be greater than about 30% w/w of total starch. Known barley plants considered to be high amylose have a content of 35-45%. The present invention however provides for barley with an amylose content that is greater than 50%, with is a level never before found in unmodified starch derived from barley.

The relative amylose content might be greater than 60% and more preferably, still greater than 70%. It may be desired to have even higher levels and thus it has been possible to achieve even higher levels in other plants by breeding with single mutations, such levels approach 90%. Thus the invention might encompass amylose levels of greater than 80% or greater than 90%.

In a fourth preferable form the starch also has an altered structure which gives rise to the resistant starch. This might arise from a high amylose content. Resistant starch might also arise because β-glucan is present at elevated levels and is likely to exert protective effects by reason of the association of the β glucan with the starch granule, the intimacy of association potentially provides a protective effect to the starch to thereby provide for a resistance that might be characterised as an RS1 form, being somewhat inaccessible to digestion. Similarly the presence of starch-lipid association as measured by V-complex crystallinity is also likely to contribute to the level of resistant starch. In this case the resistance is likely to arise because of the physically inaccessible of the starch by virtue of the presence of the lipid and accordingly this might be regarded as an RS1 starch. It is known that retrograded starch that takes up the V-complex configuration is highly resistant to digestion and accordingly it is anticipated that amylopectin that forms part of the V-complex crystalline structure will also be resistant to digestion. The starch of the exemplified barley plant may be resistant to digestion by reason of the structure of the starch granule and accordingly may have RS2 starch. Each of these characteristics might be present separately or as two or more of these characteristics in combination.

The elevated dietary fibre may at least in part take the form of resistant starch which may be characterised by a high amylose content of the starch granules as referred to above.

The relative amylose content might be greater than 60% and more preferably greater than 70%. It may be desired to have even higher levels and thus it has been possible to achieve even higher levels in other plants by breeding with single mutation such levels approach 90%. Thus the invention might encompass amylose levels of greater than 80% or greater than 90%.

It might be desired that the barley plant additionally expresses an altered level of activity of one or more amylose synthesis enzymes or other enzymes to further enhance the relative level of amylose. Thus the barley plant may carry another mutation that further decreases or alters amylopectin biosynthesis, or a mutation or genetic background that increases amylose biosynthesis. For example the barley plant may exhibit an amylose extender genotype, such as a barley plant carrying the amol mutation. An example of such a plant is the variety known as AC38 (also known as High Amylose Glacier).

It will be understood that the relative level of amylose referred to is in relation to total starch content, and thus the remainder of the starch might be predominantly of an intermediate type of starch or it might be predominantly amylopectin or a mixture of both. In the barley analysed the elevated level of amylose results from decreased amylopectin levels, and accordingly the relative level of amylose does not result from an increased synthesis of amylose.

It is known that β glucan has the effect of slowing digestion in the small intestine simply by its presence when together with another food component. Similarly it is known that resistant molecules that have close juxtaposition with starch granules help to mask the starch and contribute to its resistance by making it physically inaccessible. Elevated levels of amylose and other forms of starch as may arise from association with lipid will be further enhanced therefore by the presence and physical juxtaposition to the starch granules. Thus there is provided a significant enhancement of the effects of the resistant starch, as well as a provision of other beneficial effects arising from high β glucan levels.

Additionally it is known that there is a dose response in terms of the beneficial effects of resistant starch and β glucan. It is proposed therefore that the increased level of β glucan together with the increased levels of resistant starch will provide enhanced health benefits.

The combination of the levels of β glucan and resistant starch of at least preferred forms of this invention have not been found before and certainly not from one source without a degree of modification or purification and thus forms of the present invention provide for a single practical source of these benefits.

Another preferred aspect of the starch is that despite the high relative amylose content it also has a low gelatinisation temperature as measured by differential scanning calorimetry. This is in contrast with the general finding that high amylose starches tend to have a raised gelatinisation temperature which introduces restrictions on the manner in which high amylose starches can be utilised. On the data shown for the exemplified barley this reduced gelatinisation temperature is not just reduced when compared to starch produced by lines with somewhat elevated amylose content but also when compared with starch produced from barley with starch having normal levels of amylose. Thus whilst a preferred aspect of the invention contemplates reduced gelatinisation temperatures relative to corresponding high amylose starch it may also contemplate a gelatinisation temperature reduced relative to that of starch with normal amylose levels. For high amylose starches aspects of processing requiring higher temperatures and therefore inherently require a higher energy input which is expensive and can destroy the functionality of other food components. Similarly from the point of view of the ultimate consumer, high amylose starch foods may be less convenient because of a higher temperature or longer time required for preparation. Thus, for example, in this preferred form of the invention it is now possible to provide for a product such as a noodle product requiring the addition of boiling or heated water to a vessel such as a cup and not requiring heating for an extended period of time and at the same time providing for delivery of resistant starches and other constituents of nutritional value to the large bowel.

A major effect of the low gelatinisation temperatures of these starches is the lower temperature requirements and hence comminution energy requirement of the food. A corollary is also that where, as typically might be the case in certain food processing, mixing occurs at room temperature and then the mixture is heated, the lower gelatinisation temperature also reduces the time required to achieve gelatinisation. Additionally at a range of temperatures below the temperature for full gelatinisation of normal starch, there will be more complete gelatinisation of the starch of the present invention than normal starch.

One measure of the gelatinisation capacity is reflected in the thermal properties as measured by DSC (differential scanning calorimetry). The onset of the first peak (gelatinisation peak) of DSC may be at less than 53° C., more preferably at less than 50° C. and most preferably at less than about 47° C. The onset of the first peak may be regarded as the onset of gelatinisation. The starch produced from the barley grain may have a first peak at less than about 60° C., more preferably at less than 55° C. and most preferably at-less than 52° C. The ΔH (enthalpy) of the first peak may be less than about 3.5, more preferably less than about 1.0 and most preferably less than about 0.5.

Another finding of the gelatinsation of flours containing the starches of this invention is that they exhibit a reduced swelling. Swelling volume is typically measured by mixing either a starch or flour with excess water and heating to elevated temperatures, typically greater than 90° C. The sample is then collected by centrifugation and the swelling volume is expressed as the mass of the sedimented material divided by the dry weight of the sample. The swelling volumes of flour from starches of waxy and normal barleys are found to be greater than about 5.5. The swelling volumes of flour made from the grain that is a high amylose grain, (AC38) is about 3.75. Whereas the grains of the mutants and crosses examined are less than 3.2, preferably less than 3.0, but generally higher than about 2.

This low swelling gelatinisation characteristic is particularly useful where it is desired to increase the starch content of a food preparation, in particular a hydrated food preparation. In the present instance it might be desired to increase the dietary fibre content of a sol or other liquid preparation where there would otherwise be a restriction on delivery of the food preparation.

This characteristic in combination with the reduced gelatinisation temperature exhibited by the present starch provides a prospect of significantly enhancing the nutritional benefits of foods where there is a requirement of rapid preparation, such as instant soups and instant noodles.

It is postulated gelatinisation temperature effects are the result of an altered amylopectin structure in the endosperm of its grain, and one measurement of this structure is the distribution of chain lengths (degrees of polymerisation) of the starch molecules following debranching by isoamylase. An analysis of the chain length of the amylopectin content of the starch of the exemplified SSII mutants showed that when debranched they have a distribution of chain length in the range from 5 to 60 that is shorter than the distribution of starch yielded by non-mutant lines upon debranching. Starch with shorter chain lengths will also have a commensurate increase in frequency of branching. Thus the starch may also have a distribution of shorter amylopectin chain lengths. The proportion of starch chains that have a degree of polymerisation that falls in the range of 6 to 11 residues may be greater than 25%, more preferably greater than 30% and most preferably greater than 35%. The proportion of starch chains that have a degree of polymerisation that falls in the range of 12-30 residues may be less than 65%, more preferably less than 60% and most preferably less than about 55%. The proportion of starch chains that have a degree of polymerisation that falls in the range of 31-60 residues may be less than about 10%, more preferably less than about 8% but also preferably greater than about 5% and more preferably greater than about 6%. Rather than taken individually combination of proportions of the three chain length ranges might be taken as an indicator that a starch is of a type that accords with the present invention.

The reduction in chain length distribution is likely to contribute to lower gelatinsation temperatures. Reduced chain length is also thought to enhance the organoleptic properties of the starch, in particular mouthfeel, thus perhaps contributing to a smooth product. Additionally it has been postulated that reduced amylopectin chain length might decrease the extent of amylopectin degradation, which has an impact on food quality, for example it is thought to be important in bread staling.

The starch structure in the exemplified starch is additionally shown to differ in that the degree of crystallinity is reduced compared to normal starch isolated from barley. When combined with a reduced amylopectin chain length distribution, reduced granular crystallinity may indicate that gelatinsation temperature will be lower. The reduced crystallinity of a starch is also thought to be associated with enhance organoleptic properties and as with shorter amylopectin chain length contributes to a smoother mouth feel. Thus the starch may additionally exhibit reduced crystallinity resulting from reduced levels of activity of one or more amylopectin synthesis enzymes. The proportion of starch exhibiting crystallinity may be less than about 20% and preferably less than about 15%.

A further measure of the properties of the present starch is by measuring viscosity. It is found using a Rapid Visco Analyser that the peak viscosity of the starch of this invention is significantly different to that of normal and waxy starches and high amylose starches obtained from barley. These measurements were made on wholemeal however the properties of the starch will predominate in these measurements. The normal and waxy starches have a peak viscosity of between about 900 and about 500 RVA units, known high amylose starch has a peak viscosity of greater than 200, whereas barley plants according to the present invention have a peak viscosity of less than 100 with a majority being less than about 50 in some plants as low as about 10 RVA units. It will be understood by a person skilled in the art that the parameters cited empirical units and the results cited are intended to indicate the relative performance of these starches in RVA instruments or similar instruments such as the amylograph.

In addition to reduced crystallinity referred to above the present starch may be characterised by the presence of the V-complex form of starch. It is thought by the inventors that this is the first time that this form of starch has been exhibited in appreciable amounts in starch granules of a grain. This form of starch is usually associated with retrograded starch, in particular where there has been contact with lipids. In the case of the present invention it is postulated that the structure of the starch permits the formation of an intimate relationship between plant lipids and starch which results in the V-complex structure. It is thought that this form of starch may have health benefits because it has reduced digestibility and therefore may contribute to resistant starch.

Other forms of structure can also result from lipid-starch interaction and include non crystalline lipid-starch complexes. Thus the invention might also be said to reside in a barley plant exhibiting appreciable amounts of starch-lipid complexes in the starch content of the endosperm of its grain resulting from reduced levels of activity of one or more amylopectin synthesis enzymes. Starches that contain starch lipid complexes, including those that exhibit V-complex structure, are also usually resistant to digestion and thus contribute to the dietary fibre levels. Preferably the proportion of crystalline starch exhibiting a form of crystallinity characteristic of a starch-lipid complex is greater than about 50% and more preferably greater than about 80%.

The starch additional to the presence of the V-complex form of starch may also exhibit no appreciable amounts of A complex forms of starch. Absence of A-complex might be taken as indicator of the presence of a starch of this invention.

It is also found that the pasting temperature of strchs and product made from the grain of thisinvention are considerably elevated. The pasting temperatures in known starches is less than 70° C., and this is for both normal and high amylose starches. The starches of the present invention however preferably exhibit pasting temperatures of higher than about 75° C. or more preferably higher than about 80° C. It will be noted that these are empirical measures and might be taken as relative to those measurement of the other starches.

The starch of the exemplified barley plant is found to have significant amounts of dietary fibre and resistant starch, presumably this increase is at least in part as a result of the high relative level of amylose, however there may also be a contribution of dietary fibre by reason of starch/lipid complexes, including V-complex, or because of the intimate associate of amylose or amylopectin with β glucan. Similarly simply the elevated level of β glucan may also make a significant contribution to the elevation of dietary fibre.

The elevated relative amylose levels in the endosperm of the exemplified barley plant in all likelihood results from altered amylopectin production as a result of a reduction in the level of activity of the SSII enzyme.

Mutations in the gene encoding this enzyme might be expected to exhibit increased amylose content and/or a decrease in the level of amylopectin. Where amylopectin synthesis alone is decreased, starch exhibits an increased relative level of amylose.

Reduced activity of the amylopectin synthesis enzyme may be achieved by the appropriate mutations within a respective gene or regulatory sequences of the gene. The extent to which the gene is inhibited will to some degree determine the characteristics of the starch made. The exemplified mutations of this invention being SSII mutations in barley are truncation mutants and these are known to have a significant impact on the nature of the starch, however an altered amylopectin structure will also result from a leaky mutant that sufficiently reduces amylopectin synthesis enzyme activity to provide the characteristic of interest in the starch or grain of barley. Other chromosomal rearrangements may also be effective and these might include deletions, inversions, duplication or point mutations.

Such mutations can be introduced into desirable genetic backgrounds by either mutagenizing the varieties of interest, but more reliably by crossing the mutant with a plant of the desired genetic background and performing a suitable number of backcrosses to cross out the originally undesired parent background. Isolation of mutations might be achieved by screening mutagenised plants.

A molecular biological approach might be taken as an alternative to conventional methods. The SSII sequence is presented in this specification. Vectors carrying the desired mutations and a selectable marker may be introduced into tissue cultured plants, or suitable plant systems such as protoplasts. Plants where the mutation has been integrated into a chromosome to replace an existing wild type allele can be screened by, for example, using a suitable nucleic acid probe specific for the mutation and phenotypic observation. Methods for transformation of monocotyledonous plants such as barley and for regeneration of plants from protoplasts or immature plant embryos are well known in the art, see for example, Canadian Patent Application 2092588 by Nehra, Australian Patent Application No 61781/94 by National Research Council of Canada, Australian Patent No 667939 by Japan Tobacco Inc., International Patent Application PCT/US97/10621 by Monsanto Company, U.S. Pat. No. 5,589,617, and other methods are set out in Patent specification WO99/14314.

Other known approaches to altering the activity of the amylopectin synthesis enzyme, other than the use of mutations may also be adopted. Thus, for example, this could be by expression of suitable antisense molecules that interfere with the transcription or processing of the gene or genes encoding the amylopectin synthesis enzyme. These might be based on the DNA sequence elucidated herein for the barley SSII gene. These antisense sequences can be for the structural genes or for sequences that effect control over the gene expression or splicing event. These sequences have been referred to above. Methods of devising antisense sequences are well known in the art and examples of these are can be found in, for example, U.S. Pat. No. 5,190,131, European patent specification 0467349 AI, European patent specification 0223399 AI and European patent specification 0240208, which are incorporated herein by reference to the extent that they provide methods for carrying out antisense techniques. Methods of introducing and maintaining such sequences in plants are also published and known.

A variation of the antisense technique is to utilise ribozymes. Ribozymes are RNA molecules with enzymic function that can cleave other RNA molecules at specific sites defined by an antisense sequence. The cleavage of the RNA block the expression of the target gene. Reference is made to European patent specification 0321201 and specification WO 97/45545.

Another molecular biological approach that might also be used is that of co-suppression. The mechanism of co-suppression is not well understood, but it involves putting an extra copy of a gene into a plant in the normal orientation. In some instances the additional copy of the gene interferes with the expression of the target plant gene. Reference is made to Patent specification WO 97/20936 and European patent specification 0465572 for methods of implementing co-suppression approaches.

A further method that might be employed using the DNA sequences is duplex or double stranded RNA mediated gene suppression. In this method a DNA is used that directs the synthesis of a double stranded RNA product. The presence of the double stranded molecule triggers a response from the plant defence system that destroys both the double stranded RNA and also the RNA coming from the target plant gene, efficiently reducing or eliminating the activity of the target gene. Reference is made to Australian Patent specification 99/292514-A and Patent specification WO 99/53050 for methods of implementing this technique.

It will be understood that the invention may arise as a result of reducing the levels of activity of two or more of the above genes using a molecular biological approach.

One important product that might be envisaged in particular as a result of the high amylose and high β glucan content is a low calorific product with a reduced glycaemic index. A low calorific product might be based on inclusion of flour produced from milled grain. It might be desired, however, to first pearl the grain removing perhaps 10% or 20% by weight of the grain, thereby removing the aleurone layer and at the greater reduction removing also the germ. The effect of the pearling step is to reduce the lipid content and therefore reducing the calorific value of the food. Such foods will have the effect of being filling, enhancing bowel health, reducing the post prandial serum glucose and lipid concentration as well as providing for a low calorific food product. Use of the pearled product would result in a reduction in nutritional benefits provided by the aleurone layer and the germ. The flour produced from the pearled product is likely to have an enhanced appearance because a product made in that way tends to be whiter.

Aspects of this invention also arise from the combination of aleurone layer and germ in combination with high levels of dietary fibre. Specifically this arises from the somewhat higher relative levels of aleurone or germ present in the exemplified grain. Firstly, barley has a significantly higher aleurone layer than other commercial grains, being a result of having a three cell aleurone layer. Secondly, the exemplified barley grain is also shrunken which means that the endosperm is present in reduced amounts, a corollary of which is that the aleurone layer and the germ are present in elevated relative amounts. Thus the barley has a relatively high level of certain beneficial elements or vitamins in combination in a resistant starch delivery system, such elements include divalent cations such as bioavailable Ca⁺⁺ and vitamins such as folate or antioxidants such as tocopherols and tocotrienols. Thus calcium is established in the provision of material for growth and deposition of bone and other calcified tissue and in lowering the risk of osteoporosis later in life. Folic acid is found to be protective against neural tube defects when consumed periconceptually and decreases the risk of cardiovascular disease thereby enhancing the effects of the combination of resistant starch and β-glucan. Folic acid also is thought to have an effect of lowering the risk of certain cancers. Tocopherol and tocotrienols carry the benefits of antioxidants and are believed to lower the risk of cancer and heart disease, and also have the effect of reducing the undesirable effects of oxidation of components of a food such as fatty acids which can result in rancidity. When these components of this preferred form of barley grain or products made therefrom constitute a convenient packaging with the one grain. One specific form of milled product might be one where the aleurone layer is included in the milled product. Particular milling process might be undertaken to enhance the amount of aleurone layer in the milled product. Such a method is referred to in Fenech et al., ((1999) J Nutr 129:1114-1119). Thus any product derived from grain milled or otherwise processed to include aleurone layer and germ will have the additional nutritional benefits, without the requirement of adding these elements from separate sources.

It will be understood that the barley plant of the present invention is preferably one having grain that is useful for food production and in particular for commercial food production. Such a production might include making of flour or other product that might be an ingredient in commercial food production. A lower level of usefulness might be a starch content greater than about 12% or perhaps greater than about 15%. Or similarly this might include the capacity to mill the grain; thus whilst pearled barley may be produced from most forms of grain certain configurations of grain are particularly resistant to milling. Another characteristic that might have an impact on a variety producing a commercially useable grain is discolouration of the product produced. Thus where the husk or other portion of the grain exhibits significant colouration, for example purple, this will come through with the product and limits its commercial applications to niche applications such as being a component of a bread containing coloured whole or kibbled grains. It is generally also more convenient that the barley plants are naked, because the presence of husks on barley grains introduces greater difficulty in processing the grain. Another aspect that might make a barley plant of higher value is on the basis of starch extraction from the grain, the higher extraction rates being more useful. Grain shape is also another feature the can impact on the commercial usefulness of a plant, thus grain shape can have an impact on the ease or otherwise with which the grain can be milled, thus for example the barley grain of MK6827 plant has an unusually very elongated grain morphology which makes it difficult to mill and process. A convenient measure of this elongate shape and useability is the ratio of two morphological characteristics length of the grain to the thickness of the grain (L/T ratio). This ratio is often dictated by the nature of the starch. It has been found by the inventors that MK6827 has a L/T ratio of greater than 6. Barley plants thus screened carrying the mutant SSII gene have an L/T ratio ranging from about 4 to about 5, although it is anticipated that this might extend over an even greater range and still be useful, perhaps being less than about 5.8 or at least 5.5.

The desired genetic background will include considerations of commercial yield and other characteristics. Such characteristics might include whether it is desired to have a winter or spring type of barley, agronomic performance, disease resistance and abiotic stress resistance. In Australia one might want to cross into barley cultivars such as Sloop, Schooner, Chebec, Franklin, Arapiles, Tantangara, Galleon, Gairdner or Picola. The examples provided are specific for an Australian production region, and other varieties will be suited for other growing regions.

A fuller grain may be desirable in terms of achieving greater yields and certain benefits of the invention might be achieved, such as the production of starch with high levels of amylose, or in the alternative starch with altered chain length distributions. Other aspects of the invention may, however, be better achieved by a grain that is less filled. Thus the proportion of aleurone layer or germ to starch may be higher in less filled grain, thereby providing for a barley flour or other product that is higher in the beneficial constituents of the aleurone layer. The high aleurone layer product might thus be higher in certain vitamins such as folate, or it might be higher in certain minerals such as calcium, and that combined with higher resistant starch levels and/or higher β glucan levels might provide synergistic effects such as providing for enhance uptake of minerals in the large bowel.

In order to maximise the amount of amylose it may be desirable for the barley plant to also have other phenotypic characteristics in addition to a reduced activity of one or more amylopectin synthesising enzymes. The genetic background might therefore include additionally an high amylose phenotype for example the amol mutation in AC38 (causal gene unknown) and the waxy mutation (found for example in the Waxiro variety). Additionally it might be desired to make double mutations in other barley mutants available with shrunken endosperms where the causal gene is not known.

In a further aspect the invention could be said to reside in the grain produced from a barley plant as referred to in this specification.

It will also be understood that the invention encompasses a processed grain including a milled, ground, kibbled, pearled or rolled grain or product obtained from the processed or whole grain of the barley plant referred to above, including flour. These products may be then used in various food products, for example farinaceous product such as breads, cakes biscuits and the like, or food additives, such as thickeners or to make malted or other barley drinks, noodles and quick soups.

Alternatively the invention encompasses starch isolated from the grain of the barley plant referred to above. Starch might be isolated by known techniques.

It will be understood that one benefit of the present invention is that it provides for one or more products that are of particular nutritional benefit, and moreover it does so without the need to modify the starch or other constituents of the barley grain.

However it may be desired to make modifications to the starch, β glucan or other constituent of the grain, and the invention encompasses such a modified constituent.

The method of modification are those known, and include the extraction of the starch or β glucan or other constituent by conventional methods and modification of the starches to for the desired resistant form.

Thus the starch or β glucan may be modified either singly of multiply though the use of a treatment selected from group including but not limited to, heat and/or moisture, physically (for example ball milling), enzymatically (using for example α or β amylase, pullalanase or the like), chemical hydrolysis (wet or dry using liquid or gaseous reagents), oxidation, cross bonding with difunctional reagents (for example sodium trimetaphosphate, phosphorous oxychloride), or carboxymethylation.

The dietary fibre content of the exemplified barley grain does not result solely from the increased relative endospermal amylose content. One primary reason is that β-glucan is present at elevated levels and contributes significantly to the dietary fibre level. There are also likely to be protective effects by reason of the association of the β glucan with the starch granule, the intimacy of association potentially provides a protective effect to the starch to thereby provide for a resistance that might be characterised as an RS1 form, being somewhat inaccessible to digestion. Similarly the presence of starch-lipid association as measured by V-complex crystallinity is also likely to contribute to the level of resistant carbohydrate. In this case the resistance is likely to arise by reason of physical inaccessibility by reason of the presence of the lipid and accordingly this might be regarded as an RS1 starch. Thus it is known that retrograded starch that takes up the V-complex configuration is highly resistant to digestion and accordingly it is anticipated that amylopectin that forms part of the starch granule having the V-complex crystalline structure will have enhanced resistance to digestion. Thirdly the starch of the exemplified barley plant may be resistant to digestion by reason of the structure of the starch granule and accordingly may have RS2 starch.

It will be understood that whilst various indications have been given as to aspects of the present invention, the invention may reside in combinations of two or more aspects of the present invention.

EXAMPLE 1

Background

The synthesis of starch in the endosperm of higher plants is carried out by a suite of enzymes that catalyse four key steps. Firstly, ADPglucose pyrophosphorylase activates the monomer precursor of starch through the synthesis of ADPglucose from G-1-P and ATP. Secondly, the activated glucosyl donor, ADPglucose, is transferred to the non-reducing end of a pre-existing α1-4 linkage by starch synthases. Thirdly, starch branching enzymes introduce branch points through the cleavage of a region of α1,4 linked glucan followed by transfer of the cleaved chain to an acceptor chain, forming a new α1,6 linkage. Finally, genetic studies demonstrate that starch debranching enzymes are essential for the synthesis of normal quantities of starch in higher plants, however, the mechanism through which debranching enzymes act is unresolved (Myers et al., 2000).

While it is clear that at least these four activities are required for normal starch granule synthesis in higher plants, multiple isoforms of each of the four activities are found in the endosperm of higher plants and specific roles have been proposed for individual isoforms on the basis of mutational analysis (Wang et al, 1998, Buleon et al., 1998) or through the modification of gene expression levels using transgenic approaches (Abel et al., 1996, Jobling et al., 1999, Scwall et al., 2000). However, the precise contributions of each isoform of each activity to starch biosynthesis are still not known, and it is not known whether these contributions differ markedly between species. In the cereal endosperm, two isoforms of ADPglucose pyrophosphorylase are present, one form within the amyloplast, and one form in the cytoplasm (Denyer et al., 1996, Thorbjornsen et al., 1996). Each form is composed of two subunit types. The shrunken (sh2) and brittle (bt2) mutants in maize represent lesions in large and small subunits respectively (Girouz and Hannah, 1994). Four classes of starch synthase are found in the cereal endosperm, an isoform exclusively localised within the starch granule, granule-bound starch synthase (GBSS), two forms that are partitioned between the granule and the soluble fraction (SSI, Li et al., 1999a, SSII, Li et al., 1999b) and a fourth form that is entirely located in the soluble fraction, SSIII (Cao et al, 2000, Li et al., 1999b, Li et al, 2000). GBSS has been shown to be essential for amylose synthesis (Shure et al., 1983), and mutations in SSII and SSIII have been shown to alter amylopectin structure (Gao et al, 1998, Craig et al., 1998). No mutations defining a role for SSI activity have been described.

Three forms of branching enzyme are expressed in the cereal endosperm, branching enzyme I (BEI), branching enzyme IIa (BEIIa) and branching enzyme IIb (BEIIb) (Hedman and Boyer, 1982, Boyer and Preiss, 1978, Mizuno et al., 1992, Sun et al., 1997). In maize and rice, high amylose phenotypes have been shown to result from lesions in the BEIIb gene (Boyer and Preiss. 1981, Mizuno et al., 1993). In these mutants, amylose content is significantly elevated, and the branch frequency of the residual amylopectin is reduced. In addition, there is a significant pool of material that is defined as “intermediate” between amylose and amylopectin (Boyer et al., 1980, Takeda, et al., 1993). Mutations defining the roles of BEIIa and BEI have yet to be described, although in potato down regulation of BEI alone causes minimal affects on starch structure (Filpse et al., 1996). However, in potato the combination of down regulation of BEII and BEI provides a much higher amylose content than the down-regulation of BEII alone (Schwall et al., 2000). Two types of debranching enzymes are present in higher plants and are defined on the basis of their substrate specificities, isoamylase type debranching enzymes, and pullulanase type debranching enzymes (Myers et al., 2000). Sugary-1 mutations in maize and rice are associated with deficiency of both debranching enzymes (James et al., 1995, Kubo et al., 1999) however the causal mutation maps to the same location as the isoamylase-type debranching enzyme gene. In the Chlamydomonas sta-7 mutant (Mouille et al., 1996), the analog of the maize sugary-1 mutation, isoamylase activity alone is down regulated.

Known variation in barley starch structure is limited relative to the variation available in maize. The most highly characterised mutations are waxy and a high amylose mutation identified as AC38. Double mutants have also been constructed and analysed (Schondelmaier et al., 1992, Fujita et al, 1999). A broad range of characteristics of the variation in starch structure and properties (Czuchajowska et al., 1992; Schondelmaier et al., 1992; Vasanthan and Bhatty, 1995; Morrison et al., 1984; Gerring and DeHaas, 1974; Bankes et al., 1971; Persson and Christerson, 1997; Vasanthan and Bhatty, 1998; Czuchajowska et al., 1998; Song and Jane, 2000; Andreev et al., 1999; Yoshimoto et al., 2000), and grain properties (Swantson 1992, Ahokas 1979; Oscarsson et al, 1997; Oscarsson et al., 1998; Andersson et al., 1999; Elfverson et al., 1999; Bhatty 1999; Zheng et al., 2000; Izydorczyk et al., 2000; Andersson et al., 2000), have been reported and the utility of the mutants in animal feeding trials (Xue et al., 1996; Newman et al., 1978; Calvert et al., 1976; Wilson et al., 1975; Sundberg et al., 1998; Bergh et al., 1999), human foods (Swanston et al., 1995; Fastnaught et al., 1996; Persson et al., 1996; Pomeranz et al., 1972) and human nutrition investigated (Pomeranz 1992; Granfeldt et al., 1994; Oscarsson et al., 1996; Akerberg et al., 1998.)

In the present example, we have isolated a novel class of high amylose mutant from barley. The mutant lines contain amylose contents (65-70%) above those known from the well characterised High Amylose Glacier (AC38) mutant (45-48%)(Walker et al., 1968), and have starch with an amylopectin structure that has an increase in starch branch frequency, this is in contrast to the reduced branch frequency associated with the amylose extender mutant in maize (Takeda, et al., 1993).

The grain and starch characteristics of the present mutant have been investigated in detail and the causal mutation mapped. The mutations isolated are allelic to the previous known shrunken mutant in barley, sex6, and the causal mutation has been shown to be located within the starch synthase II gene. The effects of this mutation shed new light on the process of starch biosynthesis and illustrate how mutations in specific genes can have differing impacts on starch structure from one species to another.

Materials and Methods

Mutagenesis and Screening

The hull-less barley variety “Himalaya” was mutagenised using sodium azide according to Zwar and Chandler (1995). Selection of variants with altered grain morphology was carried out according to Green et al., (1997). A total of 75 lines with shrunken endosperm phenotypes were identified and maintained according to Green et al., (1997).

Starch Isolation

Starch was isolated from barley grain using the method of Schulman et al. (1991).

Methods for Amylose Determination

Determinations of the amylose/amylopectin ratio by an HPLC method for separating debranched starches, and an iodine binding method, were carried out as described by Batey and Curtin, (1996). Analysis of the amylose/amylopectin ratio by the analysis on non-debranched starches was carried out according to Case et al., (1998).

Starch Content Measurement

Starch was determined using the total starch analysis kit supplied by Megazyme (Bray, Co Wicklow, Republic of Ireland).

Protein Content

Nitrogen was determined by the Kjeldahl method, and protein contents were calculated using a factor of 5.7.

β-Glucan Levels

β-Glucan was determined using the kit supplied by Megazyme (Bray, Co Wicklow, Republic of Ireland).

Starch Chain Length Distribution

Starches were debranched and chain length distributions analysed using flurophore assisted carbohydrate electrophoresis (FACE) using a capillary electrophoresis according to Morell et al (1998).

DSC

Gelatinisation was measured in a Pyris 1 differential scanning calorimeter (Perkin Elmer, Norwalk Conn., USA). Starch was mixed with water in the ratio of 2 parts water: 1 part starch and this mixture (40-50 mg, accurately weighed) was placed in a stainless steel pan and sealed. The sample was scanned at 10° C. per minute from 20° C. to 140° C. with an empty stainless steel pan as a reference. Gelatinisation temperatures and enthalpy were determined using the Pyris software.

RVA Analysis

Viscosity was measured on a Rapid-Visco-Analyser (RVA, Newport Scientific Pty Ltd, Warriewood, Sydney) using conditions as a reported by Batey et al., 1997 for wholemeal flours. In order to inhibit α-amylases, silver nitrate was included in all assays at a concentration of 12 mM. The parameters measured were peak viscosity (the maximum hot paste viscosity), holding strength, final viscosity and pasting temperature. In addition, breakdown (peak viscosity minus holding strength) and setback (final viscosity minus holding strength) were calculated.

Flour Swelling

Flour swelling volume was determined according to the method of Konik-Rose et al (2001).

X-Ray Data

X-ray diffraction data was collected using standard techniques (Buleon et al., 1998).

Scanning Electron Microscopy

Scanning electron microscopy was carried out on a Joel JSM 35C instrument. Purified starches were sputter coated with gold and scanned at 15 kV at room temperature.

Doubled Haploid Production

Doubled haploids were produced from F1 plants derived from crosses between 292 and Hordeum vulgare cv Tantangara, and between 342 and H. vulgare cv Tantangara by Dr P. Davies, Waite Institute, Adelaide, Australia.

Linkage Analysis

Genetic linkage data was calculated using MapManager.

Construction of Barley cDNA Library

Five mgs of polyA+ mRNA from 10, 12 and 15 days post-anthesis of barley endosperm tissues was used for cDNA synthesis according to the protocols (Life Technology). The NotI-(dT)18 primer (Pharmacia Biotech) was used for the first stand of cDNA synthesis. The double strand cDNAs were ligated with a SalI-XhoI adapter (Stratagene) and cloned to the SalI-NotI arms of ZipLox (Life Technology) after digestion of cDNAs with NotI followed by size fractionation (SizeSep 400 spun Column of Pharmacia Biotech). The ligated cDNAs were packaged with Gigapack III Gold packaging extract (Stratagene). Titre of the library was 2×10⁶ pfu tested with Y1090(ZL) strain of E.coli.

Cloning of Specific cDNA Regions of Barley Starch Synthase II Using PCR

The cDNA clone, wSSIIp1, was used for the screening of a cDNA library of barley. The cDNA clone, wSSIIp1 was generated by PCR using the primers ssIIa (TGTTGAGGTTCCATGGCACGTTC SEQ ID NO 11) and ssIIb (AGTCGTTCTGCCGTATGATGTCG SEQ ID NO 12), amplifying the region between nucleotide positions 1,435 and 1,835 of wSSIIA (GenBank accession no: AF155217).

The amplification was performed using a FTS-1 thermal sequencer (Corbett, Australia) for 1 cycle of 95° C. for 2 minutes; 35 cycles of 95° C. for 30 seconds, 60° C. for 1 minutes, 72° C. for 2 minutes and 1 cycle of 25° C. for 1 minute. The fragment wSSIIp1 was cloned into a pGEM-T vector (Promega)

Screening of Barley cDNA Library

A cDNA library, constructed from RNA from the endosperm of barley cv Himalaya, was screened with a 347-bp cDNA fragment, wSSIIp1 at the hybridisation conditions as previously described (Rahman et al., 1998). Hybridisation was carried out in 50% formamide, 6×SSPE, 0.5% SDS, 5× Denhardt's and 1.7 μg/mL salmon sperm DNA at 42° C. for 16 h, then washed 3× with 2×SSC containing 0.1% SDS at 65° C. for 1 h per wash.

Screening of a Barley Genomic Library.

A barley (barley cv Morex) genomic library was constructed and screened essentially as described in Gubler et al (2000) using the barley SSII cDNA as a probe.

Sequencing of Genomic Clones

The Morex SSII gene was subcloned into plasmid vectors and sequenced. The 292 and MK6827 genes were sequenced by PCR amplification of overlapping regions of the gene using primers designed on the basis of the Morex sequence. PCR fragments were either sequenced directly or subcloned and sequenced from plasmids

Identification of Expressed Regions

Regions of the 292 and MK6827 genomic sequences predicted to be present in cDNAs were defined by reference to the Himalaya cDNA sequence and Morex genomic sequence.

PCR Analysis of the G to A Mutation in the SSII Gene

PCR primers were designed that amplify the region containing the G to A transition mutation identified in 292. The primer sequences are: ZLSS2P4 (CCTGGAACACTTCAGACTGTACG SEQ ID NO 13) and ZLBSSII5 (CTTCAGGGAGAAGTTGGTGTAGC SEQ ID NO 14). The amplification was performed using a FTS-1 thermal sequencer (Corbett, Australia) for 1 cycle of 95° C. for 2 minutes; 35 cycles of 95° C. for 30 seconds, 60° C. for 1 minutes, 72° C. for 2 minutes and 1 cycle of 25° C. for 1 minute.

SDS-PAGE Analysis of Barley Endosperm Proteins

Starch was prepared from the developing and mature endosperm of barley and wheat and the surface proteins were removed by proteinase K as described (Rahman et al,1995). Starch granule proteins were extarcted from 20 mg of starch dry wt., using 0.5 ml of an extraction buffer containing 50 mM Tris pH 6.8, 10% SDS and 10% 2-mercaptoethanol. After gelatinization by boiling for 10 min, and collection of the starch by centrifugation, 15 microliters of the supernatant was loaded on each lane.

Doubled Haploid Production

Doubled haploids were produced from F1 plants derived from crosses between 292 and Hordeum vulgare cv Tantangara, and between 342 and H. vulgare cv Tantangara by Dr P. Davies, Waite Institute, Adelaide, Australia.

Backcrossing Strategy

Crosses were made between 292 and Hordeum vulgare cv Sloop to generate F1 seed. Plants derived from the F1 seed were selfed to generate a population of F2 seed. The plants growing from these F2 seed were tested using a PCR assay and plants homozygous for the 292 mutation were backcrossed to Sloop (BC1). The F1 plants resulting from BC1 were again tested by PCR and plants heterozygous for the 292 mutation selected, and crossed back to Sloop (BC2). The F1 plants derived from BC2 were again analysed by PCR and plants heterozygous for the 292 mutation selected. These plants were either selfed to generate a BC2F2 population, or crossed again to Sloop (BC3). The F1 plants derived from BC3 were again analysed by PCR and plants heterozygous for the 292 mutation selected. These plants were selfed to generate a BC3F2 population. Plants derived from these seed were tested by PCR and plants homozygous for the 292 mutation selected for single seed descent and seed increase.

Results

Selection of Mutants

The identification of a range of mutants in the hull-less or naked barley variety “Himalaya” induced by a sodium azide treatment has been previously reported by Zwar and Chandler (1995). A group of 75 shrunken grain mutants were identified by the inventors and the amylose content of the starch from the shrunken seed was determined by HPLC (FIG. 1). Two lines, 292 and 342, were found to have amylose contents of 71 and 62.5% respectively (Table 1). The amylose contents of 292 and 342 were substantially higher than the previously well characterised AC38 line (47% amylose, see Table 1). This study defines the genetic basis of the novel high amylose phenotype displayed by 292 and 342, and describes effects of the causal mutation on grain and starch structure and functionality.

Grain Characteristics

Grain Size and Morphology:

The effects of the mutation on grain weight and morphology are marked (Table 2). The grain weight is reduced from 51 mg for the parent line Himalaya, to 32 mg for 292 and 35 mg for 342. The mutants retain the length and width of the wild type, but in comparison are flattened (from 2.82 mm average thickness in Himalaya to 1.58 and 1.75 mm in 292 and 342 respectively) and have an essentially unfilled central region. FIG. 2 shows photographs of the mutant and wild-type grain. The dimensions of the grain were routinely measured, the length of the grain (L), the width of the grain at the widest point (W), and the thickness (T) as indicated in FIG. 2. The ratio of length (L) to thickness (T) of the grain is a useful diagnostic for the mutation, with values of >3.5 typically found for seed carrying the 292 or 342 mutations, and values <3.5 for non-mutant barleys.

Grain Composition:

The starch content of the mutant lines is reduced from 49.0% for Himalaya to 17.7 and 21.9% for 292 and 342 respectively (see Table 1). Subtraction of the starch weight from total grain weight to give a total non-starch content of the grain, showed that the loss of starch content accounted for the loss of grain weight, with non-starch weights of 26.0, 26.3 and 27.3 mg for Himalaya, 292 and 342 respectively.

The protein content of 292 and 342 is increased relative to the parent line, Himalaya (Table 1) however, this effect is due to the loss of starch from the grain and is not due to any increase in protein synthesis per caryopsis.

The β-glucan levels of the 292 and 342 mutants are also increased, and are higher than would be expected from the effect of the reduction of starch content (Table 1). In both cases, β-glucan content is increased about 20% per caryopsis, possibly representing diversion of a small proportion of incoming carbon from starch synthesis to β-glucan synthesis.

Starch Composition and Functionality

Amylose and Amylopectin Content

Amylose content was determined using two techniques, firstly, size exclusion HPLC in 90% (v/v) DMSO, and secondly, iodine blue value. The amylose contents determined by each method were similar and the HPLC data are given in Table 1.

From grain weight and amylose content data for mutant and wild type lines, calculations of the amount of amylose deposited per grain can be made. This analysis shows that there is a decrease in amylose amount per grain from 6.2 mg/caryopsis in Himalaya, to 4.0 mg/caryopsis in 292 and 4.8 mg/caryopsis in 342. In contrast, there is a dramatic reduction in amylopectin synthesis per caryopsis, from 18.7 mg in Himalaya, to 1.6 mg in 292 and 2.9 mg in 342.

Chain Length Distribution

The chain length distribution of the starch following isoamylase debranching was carried out using fluorophore-assisted carbohydrate electrophoresis (FACE). The chain length distribution of the 292 and 342 mutants, and Himalaya, are shown in FIG. 3 a. FIG. 3 b shows a difference plot in which the normalised chain length distributions for the 292 and 342 mutants are subtracted from the normalised distribution of Himalaya. The percentages of chain lengths from DP 6-11, DP 12-30 and DP 31-65 have been calculated and are presented in Table 3. There is a marked shift in the 292 and 342 mutants in chain length distribution such that there is a higher percentage of chains in the region from DP6-11 compared to DP12-30.

Differential Scanning Calorimetry

The gelatinisation temperature of the mutants was investigated using differential scanning calorimetry, and the data is shown in Table 4. Both 292 and 342 yield starches that have markedly lower gelatinisation temperatures than the Himalaya starches, with respect to onset, peak and final temperatures for the gelatinisation peak. The enthalpy for the gelatinisation peak for the 292 and 342 mutants is also dramatically reduced in comparison to the wild type. The amylose/lipid peak onset temperature is also reduced for the 292 and 342 mutants, however, the enthalpy is increased, consistent with the increased amylose content of the mutants.

Starch Viscosity by RVA

RVA analysis of barley wholemeal samples was conducted in order to examine their pasting viscosity. Previous studies have shown that analysis of wholemeal samples is strongly correlated with the analysis of isolated starches (Batey et al., 1997). The analysis showed that there are major differences between the barley genotypes studied (see Table 5 and FIG. 4). Two barley varieties containing wild type starch, Himalaya and Namoi, showed typical RVA profiles in which there was a prominent peak viscosity, followed by a decline in viscosity to a holding strength, followed by an increase in viscosity as the temperature is reduced to a final viscosity. As is generally observed for barley starches, the final viscosities for the wild type starches were equivalent to, or less than, the peak viscosities (Table 5). In AC38, a prominent peak viscosity was obtained, however, because of the elevated amylose content of this line, the final viscosity obtained was higher than the peak viscosity. However, in 292, 342 and MK6827, a very different profile was obtained. No marked initial increase in viscosity corresponding to the peak viscosity in other barley starches was obtained, and therefore no value for breakdown could be calculated. The values for peak viscosity given in Table 5 for 292, 342 and MK6927 were the viscosities registered at the time of peak viscosity for Himalaya. In 292, 342 and MK6827, viscosity increased throughout the analysis to reach a final viscosity comparable to the other wholemeal samples. When normalized on the basis of starch content, the 292 and 342 starches had very high final viscosities (see Table 5).

Swelling volume is a method of measuring the properties of flour and starch that probes the behaviour of the material on exposure to heat and excess water. Increased uptake of water is measured by weighing the sample prior to and after mixing the sample in water at defined temperatures and following collection of the gelatinized material. The analysis showed that the control samples, Himalaya and Tantangara, swell to 6 to 8 times their dry weight, in contrast, 292 and 342 swell to just 2-3 times their dry weigh (Table 9).

Crystallinity

The structure of the starches was further investigated by X-ray crystallography (see Table 6 and FIG. 5). Himalaya shows the expected pattern for a cereal starch, having predominantly “A” type crystallinity, and both AC38 and Waxiro showed very similar X-ray diffraction patterns, although the levels of crystallinity were lower for AC38 and higher for Waxiro. For the 292 and 342 mutants, the X-ray diffraction pattern shifted to a mixture of V and B pattern. In addition to the shift in diffraction pattern, the amount of crystallinity was sharply reduced in the 292 and 342 mutants, to 9 and 12% respectively. This result is consistent with the low amylopectin content of the 292 and 342 starches.

Granule Morphology

Starch granule morphology was investigated using scanning electron microscopy (FIG. 6). The size and shape for granules from Himalaya (FIG. 6, panel A), waxy barley (Waxiro, FIG. 6 panel b), and AC38 (FIG. 6, panel c) were consistent with previously published observations of starch granules in normal barley lines. The morphology of “A” type starch granules in the mutant lines 292 (FIG. 6, panel d), 342 (FIG. 6, panel e), and MK6827 (FIG. 6, panel f), is clearly altered with the granules having a convoluted surface in comparison to the smooth lenticular shape of the normal barleys.

Dietary Fibre

Dietary fibre analysis was conducted according to the AOAC procedure and showed that there was an increase in dietary fibre in 292 and 342, and that this increase in dietary fibre was due to an increase in insoluble dietary fibre rather than soluble dietary fibre (Table 1), consistent with components of the dietary fibre being resistant starch and β-glucan. It is to be noted that this measure of dietary fibre is a chemically determined one which is quite distinct form the physiological measure relevant from a nutritional point of view.

Genetic Basis of the Mutation

Segregation Ratio

Crossing of the mutation to barley varieties not displaying the shrunken endosperm phenotype of 292 or 342 demonstrated that the mutation is a straightforward recessive mutation, displaying a 3 normal:1 shrunken ratio in the F2 seed of outcrossed populations, and 1 normal:1 shrunken ratio in the seed of a doubled haploid population developed following a single outcross (see Table 6). Normal is defined as seed with an L/T ratio of<3.5, shrunken seed as seed with an L/T ratio of>3.5.

Allelic Nature of Mutants

The 292 and 342 mutations were shown to be allelic through the analysis of progeny from crosses of 292 and 342. All F1 seed derived from reciprocal crosses showed grain weight and grain morphology phenotypes within the range of sizes and shapes observed for the parental 292 and 342 lines, and outside of the range of seed size and shape found for the parental Himalaya line. Furthermore, all F2 seed derived from 292×342 F1 plants showed the typical shrunken seed phenotype of the 292 and 342 mutants.

Analysis of the grain morphology and starch characteristics of a series of shrunken grain mutants available from the Barley Germplasm Collection (USDA-ARS, National Small Grains Germplasm Research Facility, Aberdeen, Id. 83210, USA) suggested that the line MK6827 (BGS31, also referred to as GSHO 2476), carrying the sex6 mutation showed a highly similar set of starch and grain characteristics to the 292 and 342 mutations. Crosses were established between 292 and MK6827 and all F1 grain showed the typical 292 phenotype with respect to grain weight and shrunken seed phenotype. F2 seed derived from the 292×MK6827 F1 plants all showed shrunken endosperm phenotype with L/T ratios of>4. In contrast, F2 seed from a cross between 292 and the commercial barley cultivar Sloop yielded a bimodal distribution showing a 3:1 segregation ratio between shrunken and filled seed (Table 6). F1 seed generated from crosses of 292 and 5 other lines with shrunken endosperm phenotypes (BGS 380, shrunken endosperm 4, 7HL (Jarvi et al., 1975); BGS 381, shrunken endosperm 5, 7HS (Jarvi et al., 1975); BGS 382, sex1, 6HL (Eslick and Ries 1976); BGS 396, Shrunken endosperm 6, 3HL (Ramage and Eslick 1975); BGS 397, Shrunken endosperm 7, not mapped, (Ramage and Eslick 1975) all yielded grain with a filled seed morphology. On this basis, the 292, 342 and MK6827 mutations are considered to be allelic, and on the basis of previously published map locations for the sex6 locus, the 292 and 342 mutations would be predicted to map to the short arm of chromosome 7H in barley, about 4 cM from the centromere (Netsvetaev, 1990, Netsvetaev and Krestinkov, 1993, Biyashev et al., 1986, Netsvetaev, 1992).

Linkage Analysis

A doubled haploid population was generated from a cross between 292 and the commercial malting barley variety, Tantangara, which contained 90 progeny lines (Table 8).

The lines were scored for seed morphology (filled versus shrunken seed), chain length distribution by FACE (percentage of chains with DP 6 to 11), seed covering (naked or husked), and for a PCR marker (see below). This data is given in Table 8. The shrunken seed character and 292 FACE distribution co-segregated precisely in this population, as would be expected if the altered grain size and shape were a consequence of altered starch deposition. The co-segregation of characters is illustrated in FIG. 8. Panel A shows the relationship between starch chain length (illustrated by the percentage of chains between DP 6 to 11) and the length to thickness ratio. The open circles indicate lines that have the PCR marker for the 292 mutation, the crosses indicate lines that carry the wild type PCR marker. There is a clear definition between the two groups of lines. FIG. 8 Panel B shows the relationship between starch chain length and seed weight, and shows that seed weight is less diagnostic for the mutation that the length to thickness ratio.

In barley the presence or absence of the husk is controlled by the nud locus located on chromosome 7H, and as Tantangara is a husked barley and 292 is a naked type, this character could be scored in the doubled haploid progeny. Analysis of the linkage between the naked/husked character and FACE data showed that in this cross the 292 mutation was mapped within 16.3 cM of the nud locus. This location is consistent with previous mapping data for the allelic sex6 mutation (Netsvetaev, 1990, Netsvetaev and Krestinkov, 1993, Biyashev et at., 1986, Netsvetaev, 1992).

Identification of the Causal Gene

The nud gene has been demonstrated to be located on barley chromosome 7H (FIG. 8, Fedak et al., 1972). In wheat, three starch synthases (GBSS, SSI and SSII), and an isoamylase-type debranching enzyme (S. Rahman, personal communication) are located on the short arm of chromosome 7, the homologous chromosome (Yamamori and Endo, 1996, Li et al., 1999a, Li et al., 1999b, Li et al., 2000). The close linkage to the nud locus suggested that the most probable candidate gene was the SSII gene. The wheat SSII gene has been cloned at the cDNA level (Li et al, 1999b; Genbank Accession No. AF155217) and at the genomic level (Li et al., personal communication), and a barley cDNA has been isolated and cloned (FIG. 9). The sequencing of barley and wheat SSII genomic sequences shows that the genes have very similar exon/intron structures, however, the lengths of the intron regions differ between sequences (FIG. 10). Comparison of the Morex genomic sequence and the sequence of a cDNA from Himalaya (FIG. 9) lead to the identification of deduced cDNA sequences from Morex, 292 and MK2827.

A G to A transition mutant was found in the SSII gene from 292 at a position that corresponds to 1829 of the alignment shown in FIG. 11. This mutation introduces a stop codon into the 292 SSII open reading frame (FIG. 12). Sequence analysis of Tantangara and Himalaya showed that both wild type genes were identical in this region and both 292 and 342 contained the same G to A transition mutation. The introduced stop codon would truncate the gene product such that the entire C-terminal catalytic domain of the starch synthase II gene would not be translated, and it is therefore highly likely that all SSII activity is abolished by this mutation.

A G to A transition was also present in MK6827, at position 242 of the alignment shown in FIG. 11 and the Himalaya cDNA sequence in FIG. 9. This mutation also introduces a stop codon into the 292 SSII open reading frame (FIG. 12) and would prevent translation of over 90% of the SSII gene, abolishing SSII activity encoded by this gene.

The G to A transition mutation in 292 disrupted a restriction site (NlaIV) in the barley SSII gene. The location of the diagnostic NlaIV site is shown in FIG. 14, panels (a) and (b). FIG. 14 c shows agarose gel electrophoresis of NlaIV digested products from barley showing that the diagnostic pattern for the 292 mutation is in 292 and 342 but not MK6827, Himalaya or Tantangara.

The PCR marker for the G to A transition was scored in the 90 lines of the 292× Tantanagara doubled haploid population and found to co-segregate precisely with the shrunken seed and FACE chain length distribution phenotypes, indicating that the 292 mutation is perfectly linked to this starch phenotype and that it is highly probable that this mutation is the causal mutation underlying the 292 phenotype. FIG. 14 d shows the analysis of lines from the 292× Tantangara doubled haploid population.

Biochemical Evidence for Loss of SSII Activity

The composition of starch biosynthetic enzymes in the mutant and normal barley lines was investigated using a range of gel electrophoresis techniques. Analysis of the soluble fraction of the developing endosperm demonstrated that all lines contained BEI, BEIIa, BEIIb, SSI and SSIII and that the content of these isoforms of BE and SS respectively were essentially unaltered. However, analysis of the starch granule indicated that several bands were missing. Firstly, SDS-PAGE analysis (FIG. 16, panel B) showed that a band of 90 kD was not present in 292, 342 or MK6827 that was present in Himalaya, Tantangara and AC38. This band was shown by immunoblotting to contain SSII (FIG. 16, panel B) and BEIIa and BEIIb. The finding that BEIIa and BEIIb are present in the soluble fraction but not the granule indicates that there has been an alteration in the distribution of these enzymes in the 292, 342 and MK6827 mutants, rather than a mutation abolishing expression. In contrast, no evidence was found for SSII expression in either the soluble or the granule fraction (FIG. 16, panels A and B), consistent with the genetic evidence directly linking the SSII mutation to the observed phenotypes in 292, 342 and MK6827.

Breeding of Lines Carrying the 292 Mutation

Two strategies have been used to transfer the 292 mutation into alternative barley genotypes.

In the first example, doubled haploid lines were generated from a cross between 292 and Tantangara. Data for seed covering, seed weight, L:T ratio, chain length distribution and SSII DNA marker status is given in Table 8. More comprehensive analysis of the composition of these lines is given in Table 9, including RVA analysis, β-glucan content and flour swelling volume. The data shows that the lines carrying the 292 mutation have significantly different RVA parameters (as exemplified by the Peak/Final Viscosity ratio), higher β-glucan content, and altered flour swelling volumes.

In the second example, the mutation was transferred by performing two backcrosses from 292 to a cultivar with normal starch properties (cv Sloop). The F2 seed from three backcross 2 F1 plants was collected for analysis. The F2 seed were categorized into seed with an L:T ratio of >3.5 and an L:T ratio of<3.5. The distribution of seeds between these classes was consistent with expectations for a single recessive gene. Flour swelling volume data for the categories of seeds derived from each plant are shown in FIG. 10 and shows that the starch swelling trait was clearly transferred through the breeding process into lines with an average of 75% Sloop background.

Discussion

We describe the isolation of novel mutants, 292 and 342, in barley that have a shrunken endosperm phenotype. Analysis of grain composition demonstrates that the shrunken phenotype is due to a significant decrease in starch content, and analysis of starch composition shows that this decrease is manifested as a high amylose phenotype that arises because of a decrease in amylopectin synthesis.

The 292 and 342 mutants possess a unique combination of grain and starch properties, in containing both increased β-glucan levels and resistant starch. The β-glucan levels of the lines are increased approximately 15% above that expected by the effect of reduced starch content, suggesting that carbon unable to be converted to starch is diverted to β-glucan synthesis. Determinations of dietary fibre levels demonstrate that the grain from the mutants have increased levels of dietary fibre, and that this increase is due to an increase in insoluble dietary fibre.

This combination of properties indicates that these mutants may have very interesting potential as components of the human diet. First, the elevated β-glucan levels suggests that the lines may be useful in lowering cholesterol through the well established action of β-glucan in reducing cholesterol levels. Secondly, the presence of resistant starch indicates that the lines may be beneficial from a bowel health perspective through the well established ability of resistant starches to promote colonic fermentation (Topping et al., 1997, Topping 1999). Thirdly, the grain composition indicates that the lines will have low energy density and that they may be slowly digested, indicating that they may contribute to the formulation of foods with a reduced glycaemic index.

The starch properties of the exemplified lines are also unique in that they combine a high amylose starch that also has a low gelatinisation temperature. This contrasts with high amylose mutations resulting from mutations in branching enzyme IIb in which gelatinisation temperature typically increases, such as the amylose extender mutation in maize (Ng et al., 1997, Katz et al., 1993, Krueger et al., 1987, Fuwa et al., 1999). While the amylose content of 292 is comparable to amylose extender lines, the structure of the amylopectin component of the starches differs dramatically (Wang et al., 1993). In 292 and 342, the chain length distribution of amylopectin shifts towards lower degree of polymerisation, whereas in amylose extender, the chain length distribution shifts towards increased degree of polymerisation. This suggests that amylopectin, rather than amylose content, is the primary determinant of gelatinisation temperature and that this effect is mediated through the strength of the interaction between the external chains of the amylopectin molecule. Similar effects were noted for a range of starches by Jane et al., 1999.

The viscosity data from the RVA analysis indicate that the starch from the SSII mutant lines is marked different from normal barleys and AC38. The SSII mutant barleys have essentially no peak of viscosity typically seen as the temperature is ramped up to 95° C. at the beginning of an RVA temperature profile. Instead, in these mutants, the viscosity increases steadily until a final viscosity if present. These data are consistent with the low amylopectin content of the granules, the low level of amylopectin crystallinity in the granule, and the low gelatinisation temperature and enthalpy observed in the diffential scanning calorimeter. A high final viscosity is reached once the amylose has been released from the granule through heating in excess water, and stirring. These RVA characteristics are unique for a cereal starch and provide a novel source of starch for food and industrial applications where low pasting viscosity yet high final viscosity is required.

The observations made on gelatinisation temperature in the DSC are reflected in results from X-ray diffraction studies. The granules of 292 and 342 have reduced levels of crystallinity and the crystal form shifts from the A type typical of cereal starches to a mixture of V and B types. The V type is typical of amylose and reflects the amylose component of the starch complexed with fatty acids, while the B form is derived from amylopectin and presumably reflects the residual amylopectin content of the starch (Buleon et al, 1998).

Analysis of the genetic basis of the 292 and 342 mutations demonstrates that the mutations are simple recessive mutations that give typical Mendelian ratios in outcrossing experiments. Crossing studies demonstrated that 292 and 342 are allelic. Further analysis of the interaction between 292 and other shrunken endosperm mutations in crossing experiments demonstrated that the 292/342 mutations were also allelic with the Sex6 mutation in the line MK6827. This mutation has previously been mapped and shown to be located within 3 cM of the centromere on the short arm of chromosome 7H (Netsvetaev, 1990, Netsvetaev and Krestinkov, 1993, Biyashev et al., 1986, Netsvetaev, 1992).

A doubled haploid population between the husked barley Tantangara and the naked 292 mutant was established and the shrunken endosperm mutation mapped to the short arm of chromosome 7HS, to within 16 cM of the nud gene, a location consistent with the map location of the Sex6 mutation.

The localisation of the gene to the region adjacent to the centromere on the short arm of chromosome 7HS demonstrates that the causal mutation (sex6) is in a different gene to the mutation that causes the high amylose phenotype in AC38 (amol) which has been mapped to chromosome 1H (Schondelmeier et al 1992). The map location suggested that one candidate for the gene disrupted in the sex6/292 mutation was starch synthase II, known in wheat to be localised in the same region of the chromosome (Yamamori and Endo 1996, Li et al, 1999b). Sequence analysis of the 292 and 342 mutants showed that there was a G to A transition mutation in the gene which would cause truncation of the gene such that the C-terminal region containing the active site of the enzyme would not be translated, presumably leading to the synthesis of a completely inactive protein. Furthermore, the sequencing of the SSII gene from MK6827 showed a G to A transition mutation at position 242 which would also cause truncation of the gene. This result confirms the allelic nature of the 292 and MK6827 mutations.

The identification of mutations in the SSII gene lead to the development of a PCR marker diagnostic for the mutation in 292. This PCR marker was scored across the 91 progeny of the 292× Tantangara population and shown to 100% co-segregate with the shrunken endosperm phenotype and the reduced chain length distribution phenotype of starch. The discovery of allelic mutations in the SSII genes from barleys of diverse backgrounds (292 and MK6827) which give rise to similar phenotypes, and the perfect linkage of the mutation to the shrunken grain phenotype provides a high degree of certainty that the mutations present in the SSII genes of 292, 342 and MK6827 are the causal mutations leading to the shrunken endosperm character.

The phenotype observed here for the SSII mutation in barley is similar to the phenotypes of SSII mutations in other plants in some respects, however, SSII mutations do not give rise to amylose contents as high as those found in 292/342. SSII mutants are known in pea (rug5, Craig et al., 1998) and Chlamydomonas (Fontaine et al., 1993) and give rise to amylopectins with reduced chain length distributions, as observed here. There is also evidence to suggest that the Shrunken-2 mutation in maize arises through mutation of the SSII gene although this has yet to be conclusively demonstrated (Ham et al., 1998, Knight et al., 1998). In maize, the Shrunken-2 mutation gives rise to starches with reduced gelatinisation temperatures (Campbell et al., 1994). In wheat, Yamamori has developed a triple null line that lacks the Sgp-1 protein (Yamamori 1998) that has been shown by Li et al (Li et al, 1999b) to be the product of the SSII gene. In wheat, amylose content is increased to about 35% and abnormal starch granules, altered crystallinity and altered gelatinisation temperature are observed (Yamamori 1998). The differences in properties between the barley SSII mutants and SSII mutants from other species are quite unexpected.

The SSII mutation has been shown to be able to be transferred by breeding from one genetic background to another and yield diagnostic grain morphology and composition typical of the original 292, 342 and MK6827. In table (9) data from 292× Tantangara doubled haploid lines for the L/T ratio, β-glucan content, chain length distribution, RVA and flour swelling volume parameters demonstrate that lines carrying the 292 mutation show phenotypes typical of the 292 parent. In a further demonstration, the segregation of seed from the selfed progeny of a second backcross of 292 to Sloop showed a segregation ratio consistent with 3:1 segregation for the normal (74 seeds with L/T ratio<3.5) and shrunken phenotypes (21 seeds L/T ratio>3.5).

The availability of the sequence of the SSII gene and barley transformation systems provides the tools required to knock out the SSII gene using gene suppression technologies, in order to produce a comparable phenotype to that found with the SSII mutations. A recently developed highly effective strategy is to produce a hairpin construct designed to produce a double stranded RNA which would suppress the endogenous SSII activity. While complete knock out mutants analogous to the mutations described here would be of interest, the use of DNA constructs with differing promoters, and the recovery of transgenes with differing levels of hairpin construct expression, would allow the impact of titrating the expression of the gene from normal levels to complete knockdown levels to be assessed.

The mutations were shown to be able to be transferred from 292 into alternative barely genetic backgrounds, while retaining essential features of the original 292 mutation. In Tables 9 and 10, phenotypic data for 292× Tantangara doubled haploid progeny, and the seed from a second backcross to Sloop, are shown, and indicate that the phenotypes are transferred through the breeding process.

TABLE 1 Barley Grain Composition Amylose Amylose Content Content by Total Insoluble Soluble Starch By iodine Protein Dietary Dietary Dietary Content HPLC binding Content β-glucan Fibre^(a) Fibre^(a) Fibre^(a) (%)^(a) (%)^(b) (%) (%)^(a) (%)^(a) (%) (%) (%) Glacier n.d. 31.0 n.d. 11.5 4.3 21.6 16.6 5   AC38 47   47.4 60.6 10.4 5.8 24.9 28.8 6.1 Himalaya 49   25   25.4 10.0 4.8 27.1 18.1 9   292 17.7 71   68.9 15.0 9.5 30.3 21.4 8.9 342 21.9 62.5 71.7 15.7 8.3 28.3 19.4 8.9 MK6827 10.2 n.d. 44.4 21.3 n.d. n.d. n.d. n.d. Waxiro 42.8 n.d.  5.0 14.6 n.d. 19.8 12.7 7.1. Tantangara 51.6 n.d. 29.5 14.6 n.d. 17.2 12.7 4.5. ^(a)% grain weight, 14% moisture ^(b)% of total starch content n.d. not determined

TABLE 2 Grain Dimensions Grain Grain Grain Length Width Thickness Grain weight (mg) (mm) (mm) (mm) L/T Ratio Himalaya 51.01 ± 6.63^(a)  7.01 ± 0.51 3.58 ± 0.34 2.82 ± 0.36 2.48 Tantangara 50.40 ± 6.51^(a)  7.22 ± 0.98 3.60 ± 0.25 2.73 ± 0.21 2.64 Waxiro 45.71 ± 5.21  7.54 ± 0.47 3.40 ± 0.20 2.67 ± 0.19 2.82 AC38 50.79 ± 8.22  7.62 ± 0.65 3.35 ± 0.27 2.64 ± 0.25 2.89 292 32.13 ± 4.67^(a)  7.05 ± 0.49 3.63 ± 0.55 1.58 ± 0.20 4.46 342 35.45 ± 6.01  7.28 ± 0.55 3.76 ± 0.38 1.75 ± 0.18 4.16 MK6827 44.89 ± 3.78 11.20 ± 0.58 3.63 ± 0.27 1.77 ± 0.33 6.33 N = 50, except where indicated by ^(a), n = 200

TABLE 3 Chain Length Distribution of Isoamylase Debranched Starches Himalaya Tantangara AC38 342 292 MK6827 Dp^(a) %^(b) %^(b) %^(b) %^(b) %^(b) %^(b) DP 24.15 22.40 26.33 38.18 38.96 37.98 6-11 DP 69.12 67.59 67.62 54.14 53.42 55.60 12-30 DP 6.73 10.01 6.05 7.68 7.62 6.42 31-60 ^(a)degree of polymerisation ^(b)percentage of distribution of oligosaccharides expressed on a molar basis

TABLE 4 Barley Starch Thermal Properties Measured by DSC Peak 1 Peak 2 Onset Peak End ΔH Onset Peak End ΔH Glacier 55.4 59.3 65.3 4.2 93.9 101.4 107.7 0.87 AC38 55.0 62.2 68.2 3.9 89.3 100.1 106.9 1.195 Himalaya 56.8 60.9 68.0 4.5 93.1 101.8 108.3 0.78 292 46.0 51.2 58.1 0.29 88.7 97.7 104.9 1.34 342 45.2 50.4 56.8 0.47 86.5 97.0 105.0 1.59

TABLE 5 RVA Parameters for Barley Starches Normalised Pasting Peak Holding Final Final Temp Viscosity Breakdown Strength Setback Viscosity Viscosity* (C.) Himalaya 871.5 653.1 218.4 235.8 454.2 926 64.9 Namoi 621.7 367.5 254.2 375.3 629.5 1284 65.9 AC38 226.7  87.3 139.4 188.4 327.8 697 68.9 292 92.1** *** 133.9 230 363.9 2055 89.5 342 110.9** *** 144.9 264.5 409.4 1869 87.9 MK6827 18.2** *** 25.7 43.3 69 676 n.d. *Final viscosity divided by starch content of wholemeal **Value registered at time of peak viscosity for Himalaya *** Value was less than zero n.d. not determined

TABLE 6 Starch Crystallinity Data % H2O Crystallinity A B V Sample (W.B) %* %* %* %* 292 29.6 9 — 13 87 342 35.8 12 — 18 81 AC38 26.1 19 93 7 (traces) Himalaya 27.7 27 93 7 (traces) Waxiro 29.7 41 94 6 — (*±5%)

TABLE 7 Progeny Analysis Cross Shrunken Full Calculated X² value^(c) 292 × Sloop^(a) 45 155 X² (3:1) = 1.0 292 × Tantangara^(b) 45  46 X² (1:1) = 0.01 ^(a)progeny from standard cross ^(b)doubled haploid progeny ^(c)in each case, X² (0.05), df = 1 = 3.84, hence the 292 × Sloop population fits a 3:1 segregation and 292 × Tantangara doubled haploid population fits a 1:1 segregation

TABLE 8 Scoring of 292 × Tantangara Doubled Haploid Lines Seed Line Weight DP6-11 Amylose Number^(a) Husk^(b) (mg) L/T Ratio^(c) (%)^(d) Content^(e) PCR^(f) 1 N 26 3.8 35.87 50.2 292 2 N 24 4.21 36.87 56.2 292 3 H 43 3.32 25.45 18.3 Wt 5 N 40 4.58 39.47 55.5 292 7 N 34 4.28 19.63 43.0 292 8 H 48 3.02 21.6 46.7 Wt 9 N 31 2.76 22.89 25.9 Wt 10 N 26 3.02 27.56 21.1 Wt 11 N 34 3.55 37.90 44.7 292 12 H 50 2.94 26.37 32.8 Wt 13 N 27 4.29 38.68 48.4 292 14 H 56 3.07 22.98 20.8 Wt 15 H 46 2.74 24.88 22.9 Wt 16 H 43 2.78 25.40 18.3 Wt 17 N 31 3.8 37.37 54.2 292 18 N 31 4.51 37.46 57.5 292 19 H 26 3.1 29.57 22.7 Wt 20 H 53 3.04 25.42 23.8 Wt 21 N 31 4.5 38.51 59.1 292 22 N 27 4.63 37.25 27.2 292 23 H 47 2.73 24.11 21.2 Wt 24 N 27 4.58 36.89 42.0 292 26 H 35 3.57 19.50 15.1 Wt 27 H 22 4.3 36.81 48.6 292 28 N 31 4.34 38.88 37.0 292 30 N 30 4.04 38.05 48.4 292 31 N 23 4.25 37.07 51.7 292 32 H 48 2.62 20.67 13.0 Wt 33 N 25 4.92 35.68 33.3 292 34 N 31 4.01 38.34 46.1 292 35 H 43 3.16 20.07 23.6 Wt 36 N 26 4.33 36.93 29.7 292 38 H 38 3.01 21.11 9.1 Wt 39 H 33 2.92 20.49 23.5 Wt 40 H 36 2.99 19.57 2.2 Wt 41 N 30 4.05 37.82 40.9 292 42 H 47 2.95 20.80 11.9 Wt 43 N 40 3.24 21.97 18.1 Wt 45 H 52 2.78 19.97 14.5 Wt 46 N 29 4.44 35.87 32.1 292 47 N 35 3.69 36.34 92.9 292 48 H 31 2.54 20.27 13.4 Wt 49 H 54 2.94 22.29 19.3 Wt 50 H 50 2.94 21.92 20.6 Wt 51 H 43 3.73 20.59 18.1 Wt 53 N 31 4.12 36.52 55.3 292 54 N 34 4.02 35.17 57.1 292 55 H 32 4.19 41.35 60.4 292 56 N 29 3.17 21.48 18.1 Wt 57 H 30 4.85 36.66 46.3 292 58 N 32 2.97 23.83 13.8 Wt 59 N 46 2.91 24.15 9.2 Wt 60 H 44 2.74 22.39 13.5 Wt 61 N 31 4.47 35.67 61.3 292 63 N 32 4.3 36.94 39.4 292 64 H 39 2.93 21.95 20.5 Wt 65 N 26 3.87 37.51 20.7 292 66 N 30 4.03 36.89 48.7 292 67 H 36 3.17 20.24 14.4 Wt 68 N 43 2.65 22.53 8.4 Wt 69 N 32 3.93 36.34 54.7 292 70 H 43 2.77 22.28 17.6 Wt 71 N 29 3.73 38.73 31.5 292 72 H 47 2.65 22.00 20.8 Wt 73 N 36 4.09 39.58 49.0 292 74 N 24 4.18 36.15 47.8 292 75 H 34 2.99 24.42 14.2 Wt 76 N 31 4.35 35.95 49.9 292 77 H 49 3.19 21.22 17.0 Wt 78 H 33 2.78 21.27 15.6 Wt 79 H 31 2.85 23.04 21.2 Wt 80 H 38 3.18 19.88 18.9 Wt 81 H 37 2.84 24.22 16.2 Wt 82 H 33 4.64 39.99 45.3 292 84 N 28 3.62 36.98 28.9 292 85 N 26 6.44 44.43 41.3 292 86 H 32 2.87 30.73 16.1 Wt 88 N 26 4.62 46.12 39.3 292 89 H 38 2.88 31.25 16.3 Wt 90 H 32 3.19 31.11 13.8 Wt 91 N 31 4.17 42.86 37.3 292 92 N 27 3.99 45.30 44.6 292 93 H 37 2.99 30.77 12.5 Wt 94 H 43 3.67 29.46 21.9 Wt 96 N 33 5.69 47.34 52.2 292 97 N 23 3.41 31.36 17.1 Wt 98 N 32 5.95 45.27 52.4 292 99 N 19 3.68 38.36 1.7 292 100 H 36 3.1 31.92 15.4 Wt 101 N 58 3.29 24.71 2.9 Wt ^(a)292 × Tantangara doubled haploid line ^(b)Husk phenotype. N, naked; H, husked ^(c)L/T ratio: length to thickness ratio ^(d)Percentage of chains in debranched starch with DP6 to DP11, calculated on a molar basis as a percentage of chains eluting between DP6 and DP65 ^(e)Amylose content determined by iodine blue value ^(f)PCR score. 292, PCR reaction yields band which yields 169 bp band plus 103 bp on NlaIV digestion; Wt, PCR reaction yields band which yields 111 bp, 103 bp and 57 bp band on NlaIV digestion

TABLE 9 Detailed Analysis of Doubled Haploid Lines RVA Peak RVA Final Viscosity Viscosity Ratio β-glucan Flour (RVA (RVA Peak/Final Content Swelling Line L/T Ratio FACE Units) Units) Viscosities (%) Volume Control Sloop 2.78 23.5 535.8 483.5 1.11 2.3 7.54 Tantangara 2.64 22.4 507 395.1 1.28 5.16 5.97 Himalaya 2.48 24.2 873.9 449.3 1.94 8.53 8.18 AC38 2.89 26.33 226.7 327.8 0.69 5.8 3.75 292 4.46 38.9 92.1 363.9 0.25 13.09 2.00 MK6827 6.33 37.98 18.2 69 0.26 n.d. 2.11 Doubled Haploid Line Wild Type  8 3.02 21.6 527.9 431.3 1.22 8.9 6.47  43 3.24 25.4 566.6 527.4 1.07 7.77 6.04  56 3.17 24.9 703.1 523.5 1.34 7.81 6.95  58 2.97 27.9 726.8 588.8 1.23 9.65 6.23  59 2.91 27.0 655 435.8 1.50 7.16 7.21  68 2.65 22.5 876.3 465.5 1.88 8.87 8.63 101 3.29 34.71 471.3 410.3 1.15 6.54 6.26 Mutant SSII  5 4.58 39.5 68.7 316.6 0.217 9.87 2.55  11 3.55 48.2 51.5 240.8 0.21 8.36 2.58  13 4.29 38.7 43.7 265.5 0.16 11.13 2.92  27 4.30 36.8 20.3 96.6 0.21 13.11 2.71  30 4.04 38.05 57.3 251.1 0.23 10.56 2.27  31 4.25 37.1 17.6 124.5 0.14 11.35 2.48  33 4.92 35.7 11.7 83.5 0.14 7.22 2.13  36 4.33 36.9 14.5 93.6 0.15 7.20 2.20  46 4.44 35.9 31.3 175.8 0.18 10.02 2.32  91 4.17 42.9 35.8 189.5 0.19 11.3 2.43 n.d. not determined

TABLE 10 Flour Swelling Data for BC2F2 seed Line Swelling Volume C5/1 Plant 1 L:T > 3.5 2.118 C5/1 Plant 1 L:T < 3.5 6.913 65/2 Plant 1 L:T > 3.5 2.382 65/2 Plant 1 L:T < 3.5 7.565 65/2 Plant 2 L:T > 3.5 2.409 65/2 Plant 2 L:T < 3.5 6.707

EXAMPLE 2

Design and Construction of Vectors

Regions of the barley SSII gene (as defined in FIG. 15) were cloned into vectors for transformation. Three constructs were prepared for each gene target, addressing the gene suppression strategies, (1) sense cosuppression, (2) antisense and (3) duplex-mediated suppression.

FIG. 16 illustrates the configuration of sequences in DNA constructs designed to suppress the expression of the endogenous target gene. The promoter may be selected from either endosperm-specific (such as High Molecular Weight Glutenin promoter, the wheat SSI promoter, wheat BEII promoter) or promoters not specific for the endosperm (such as ubiquitin or 35S). The construct may also contain other elements that enhance transcription such as the nos 3 element of OCS. The regions of DNA illustrated will be incorporated into vectors containing suitable selectable marker gene sequences and other elements, or into vectors that are co-transformed with vectors containing these sequences.

Cereal Transformation

Methods for the transformation of barley (Tingay et al., 1997; Wan et al, 1994) oats (Somers et al., 1992, 1994; Gless et al., 1998; Zhang et al., 1999, Cho et al., 1999) and rye (Castillo et al., 1994; Pena et al., 1984) have been described and can be used to transfer DNA constructs generating transgenic plants.

Analysis of Transgenics

Identification of transgenic plants is carried out through identification of the DNA of the DNA construct through PCR or through Southern hybridisation. The levels of the expression of the individual barley starch biosynthetic genes is measured at both the mRNA and protein levels through standard techniques such as Northern hybridisation and Western blotting respectively. The starch and grain content and composition is measured using standard techniques such as those exemplified in Example 1.

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1. Barley grain, comprising starch, wherein the amylose content of the starch of the barley grain is greater than 50% (w/w) of total starch content as determined by size exclusion HPLC in 90% (v/v) DMSO, and having a length to thickness ratio of less than 5.8, and having a reduced level of active starch synthase II (SSII) protein relative to the level in Himalaya variety of barley grain.
 2. The barley grain of claim 1, wherein the amylose content of the starch of the barley grain is greater than 60% (w/w) of total starch content as determined by size exclusion HPLC in 90% (v/v) DMSO.
 3. The barley grain of claim 1, comprising at least 6% β-glucan as a percentage of total non-hulled grain weight.
 4. The barley grain of claim 1, having a length to thickness ratio of less than 5.5.
 5. The barley grain of claim 4, having a length to thickness ratio in the range of 4 to
 5. 6. The barley grain of claim 1, characterized in that flour of the grain or wholemeal of the grain has a swelling volume of less than 3.2 as determined by mixing the flour or wholemeal with excess water and heating at a temperature greater than 90° C.
 7. The barley grain of claim 6, characterized in that flour of the grain or wholemeal of the grain has a swelling volume of at least
 2. 8. The barley grain of claim 1, characterized by having a starch content of greater than 12% of the naked grain, by exhibiting no purple coloration, or by being naked.
 9. The barley grain of claim 1 which is suitable for food production.
 10. The barley grain of claim 1 which is milled, ground, pearled, rolled, kibbled, cracked or whole grain.
 11. The barley grain of claim 1 which is whole grain.
 12. The barley grain of claim 1, wherein the SSII protein is encoded by a gene having a G to A transition mutation, which mutation introduces a stop codon into the SSII open reading frame.
 13. The barley grain of claim 1, wherein the starch of the grain exhibits a reduced gelatinisation temperature relative to that of starch from Himalata variety of barley grain as measured by differential scanning calorimetry.
 14. The barley grain of claim 13, wherein the reduced gelatinisation temperature is characterized by a reduced temperature of onset of the first peak detected by the differential scanning calorimetry relative to that of starch from Himalaya variety of barley grain.
 15. The barley grain of claim 14, wherein the temperature of onset of the first peak is less than 53° C.
 16. The barley grain of claim 13, wherein the reduced gelatinisation temperature is characterized by a reduced temperature of the apex of the first peak detected by the differential scanning calorimetry relative to that of starch from Himalaya variety of barley grain.
 17. The barley grain of claim 16, wherein the temperature of the apex of the first peak is less than 60° C.
 18. The barley grain of claim 13, wherein the reduced gelatinisation temperature is characterized by a reduced enthalpy (ΔH) of the first peak detected by the differential scanning calorimetry relative to that of starch from Himalaya variety of barley grain.
 19. The barley grain of claim 1, wherein the starch when gelatinized exhibits reduced peak viscosity relative to that of starch from Himalaya variety of barley grain.
 20. The barley grain of claim 1, wherein the pasting temperature of the starch is higher than 75° C.
 21. The barley grain of claim 1, wherein the grain comprises starch associated lipid, said starch and associated lipid exhibiting crystallinity comprising V-complex crystallinity, wherein greater than 10% of the starch crystallinity is V-complex crystallinity.
 22. The barley grain of claim 21, wherein the proportion of the starch of the grain that exhibits crystallinity is less than 20%.
 23. The barley grain of claim 1, wherein the starch exhibits an amylopectin chain length distribution wherein the proportion of starch chains having a degree of polymerization between 6 and 11 residues is greater than 25%.
 24. The barley grain of claim 1, wherein the barley grain is in a food product.
 25. The barley grain of claim 24, wherein the food product is a farinaceous product, bread, cake, biscuits, noodles or soup.
 26. A process for making the barley grain of claim 1, comprising the steps of: a) introducing a genetic variation into a parent barley plant, b) obtaining seed from the parent barley plant, and c) screening the seed obtained from the parent barley plant for an increased level of amylose, which level is greater than 50% (w/w) of the starch of the seed.
 27. The process of claim 26, wherein step a) comprises mutagenesis.
 28. The process of claim 26, wherein step a) comprises introducing the genetic variation by crossing.
 29. The process of claim 26, wherein step c) comprises screening the seed for a shrunken endosperm phenotype.
 30. A process for making starch comprising, a) milling the barley grain of claim 1, and b) extracting starch from the milled barley grain.
 31. A process for making a food product, comprising the steps of a) obtaining the barley grain of claim 1 as whole grain, milled, ground, pearled, rolled, kibbled, or cracked, b) processing the barley grain of step a) so as to make the food product.
 32. A process for making a food product comprising the steps of: a) milling the barley grain of claim 1, b) extracting starch from the milled barley grain, and c) including the starch from the milled barley grain in the food product.
 33. The barley grain of claim 1, wherein the amylose content of the starch of the barley grain is greater than 70% (w/w) of total starch content as determined by size exclusion HPLC in 90% (v/v) DMSO. 